Lista de obras - Stefano Squarzoni - Dominio Público Uruguay

82nd ENMC international workshop, 5th international Emery-Dreifuss muscular dystrophy (EDMD) workshop, 1st Workshop of the MYO-CLUSTER project EUROMEN (European muscle envelope nucleopathies), 15-16 September 2000, Naarden, The Netherlands

artículo científico publicado en 2002

98th ENMC International Workshop on Congenital Muscular Dystrophy (CMD), 7th Workshop of the International Consortium on CMD, 2nd Workshop of the MYO CLUSTER project GENRE. 26-28th October, 2001, Naarden, The Netherlands.

artículo científico publicado en 2002

A case report of fracture of ceramic head in total hip arthroplasty: histological and biochemical features of perimplant tissues

artículo científico publicado en 2006

A new method for isolation of polyethylene wear debris from tissue and synovial fluid

A pathogenic mechanism leading to partial lipodistrophy and prospects for pharmacological treatment of insulin resistance syndrome

artículo científico publicado en 2007

A recently developed bifacial platelet-rich fibrin matrix

scientific article published on 01 July 2010

All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype.

artículo científico publicado en 2015

Altered chromatin organization and SUN2 localization in mandibuloacral dysplasia are rescued by drug treatment.

artículo científico publicado en 2012

Altered pre-lamin A processing is a common mechanism leading to lipodystrophy.

artículo científico publicado en 2005

Antisense-induced messenger depletion corrects a COL6A2 dominant mutation in Ullrich myopathy

artículo científico publicado en 2012

Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts

artículo científico publicado en 2003

At the nucleus of the problem: nuclear proteins and disease

artículo científico publicado en 2003

Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria.

artículo científico publicado en 2011

Autosomal recessive Bethlem myopathy

artículo científico publicado en 2009

Autosomal recessive myosclerosis myopathy is a collagen VI disorder

artículo científico publicado en 2008

Barrier-to-autointegration factor (BAF) involvement in prelamin A-related chromatin organization changes

artículo científico publicado en 2015

Ceramic debris in hip prosthesis: correlation between synovial fluid and joint capsule

scientific article published on 13 March 2013

Chromosome spread for confocal microscopy

artículo científico publicado en 1999

Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts

article

Collagen VI-NG2 axis in human tendon fibroblasts under conditions mimicking injury response

article

Considerations on ceramic prosthesis explants

scientific article published on 01 October 1992

Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by collagen VI myopathies

artículo científico publicado en 2012

Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies

artículo científico publicado en 2014

Determination of crystallinity and crystal structure of Hylamer polyethylene after in vivo wear

artículo científico publicado en 2006

Differential and restricted expression of novel collagen VI chains in mouse

artículo científico publicado en 2011

Diverse lamin-dependent mechanisms interact to control chromatin dynamics. Focus on laminopathies

artículo científico publicado en 2014

Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy

artículo científico publicado en 2005

Drugs affecting prelamin A processing: effects on heterochromatin organization

artículo científico publicado en 2007

Dysferlin in a hyperCKaemic patient with caveolin 3 mutation and in C2C12 cells after p38 MAP kinase inhibition

artículo científico publicado en 2003

Early diagnosis of ceramic liner fracture. Guidelines based on a twelve-year clinical experience.

artículo científico publicado en 2006

Effect of mechanical strain on the collagen VI pericellular matrix in anterior cruciate ligament fibroblasts.

artículo científico publicado en 2014

Effects of prelamin A processing inhibitors on the differentiation and activity of human osteoclasts

artículo científico publicado en 2008

Effects on Collagen VI mRNA Stability and Microfibrillar Assembly of ThreeCOL6A2Mutations in Two Families with Ullrich Congenital Muscular Dystrophy

artículo científico publicado en 2002

Electron microscopy microsampling of isolated nuclei sorted by flow cytometry

artículo científico publicado en 1986

Emerin Phosphorylation during the Early Phase of the Oxidative Stress Response Influences Emerin-BAF Interaction and BAF Nuclear Localization

artículo científico publicado en 2020

Emerin increase in regenerating muscle fibers

article

Emerin presence in platelets

artículo científico publicado en 2000

Emerin-prelamin A interplay in human fibroblasts

artículo científico publicado en 2009

Emery-Dreifuss muscular dystrophy, nuclear cell signaling and chromatin remodeling

artículo científico publicado en 2002

Experimental colitis increases small intestine permeability in the rat

scientific article published on 01 January 1999

Expression of collagen VI α5 and α6 chains in human muscle and in Duchenne muscular dystrophy-related muscle fibrosis

artículo científico publicado en 2011

Expression of the collagen VI α5 and α6 chains in normal human skin and in skin of patients with collagen VI-related myopathies

Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutation

artículo científico publicado en 2003

Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for gene transcription

artículo científico publicado en 2003

Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistribution

artículo científico publicado en 2012

Fretting wear in a modular neck hip prosthesis.

artículo científico publicado en 1997

Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy ⬇️

artículo científico publicado el 1 de diciembre de 1997

Honey flavonoids inhibit Candida albicans morphogenesis by affecting DNA behavior and mitochondrial function

artículo científico publicado en 2014

Image analysis of the chromatin organization in the nuclear domains of freeze fractured hepatocytes and lymphocytes

scientific article published on 01 January 1990

Image analysis techniques. The problem of the quantitative evaluation of the chromatin ultrastructure

Immunocytochemical detection of emerin within the nuclear matrix

artículo científico publicado en 1998

Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology.

artículo científico publicado en 2003

Implications for nuclear organization and gene transcription of lamin A/C specific mutations

article

Increase of Neuronal Nitric Oxide Synthase in Rat Skeletal Muscle during Ageing

artículo científico publicado en 1998

Intracellular detection of laminin alpha 2 chain in skin by electron microscopy immunocytochemistry: comparison between normal and laminin alpha 2 chain deficient subjects

artículo científico publicado en 1997

Intramembrane protein distribution in cell cultures is affected by 50 Hz pulsed magnetic fields.

artículo científico publicado en 1997

Intranuclear localization of phospholipids by ultrastructural cytochemistry

artículo científico publicado en 1992

Isolation and characterization of wear debris generated in patients wearing polyethylene Hylamer inserts, gamma irradiated in air.

artículo científico publicado en 2005

Lamin A precursor induces barrier-to-autointegration factor nuclear localization

artículo científico publicado en 2010

Lamin A/C sustains PcG protein architecture, maintaining transcriptional repression at target genes.

artículo científico publicado en 2015

Laminopathies: a chromatin affair

artículo científico publicado en 2006

Laminopathies: involvement of structural nuclear proteins in the pathogenesis of an increasing number of human diseases

artículo científico publicado en 2005

Localization of laminin alpha 2 chain in normal human central nervous system: an immunofluorescence and ultrastructural study

artículo científico publicado en 1997

Localization of the laminin alpha 2 chain in normal human skeletal muscle and peripheral nerve: an ultrastructural immunolabeling study

artículo científico publicado en 1997

Metal-on-metal hip prostheses: correlation between debris in the synovial fluid and levels of cobalt and chromium ions in the bloodstream.

artículo científico publicado en 2014

Mineralization behavior with mesenchymal stromal cells in a biomimetic hyaluronic acid-based scaffold.

artículo científico publicado en 2010

Mixing and matching in ceramic-on-metal hip arthroplasty: an in-vitro hip simulator study

artículo científico publicado en 2009

Modulation of TGFbeta 2 levels by lamin A in U2-OS osteoblast-like cells: understanding the osteolytic process triggered by altered lamins

artículo científico publicado en 2015

Morphological evidence of function-related localization of phospholipids in the cell nucleus

artículo científico publicado en 1992

Morphometric and microanalytical analyses of alumina wear particles in hip prostheses

artículo científico publicado en 1993

Morphometric study of chromatin pattern in freeze-fractured rat liver nuclei during malignancy evolution

artículo científico publicado en 1989

Muscular laminopathies: role of prelamin A in early steps of muscle differentiation

artículo científico publicado en 2010

New roles for lamins, nuclear envelope proteins and actin in the nucleus

artículo científico publicado en 2004

Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy

article published in 2001

Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophy

artículo científico publicado en 1999

Nuclear envelope proteins and chromatin arrangement: a pathogenic mechanism for laminopathies.

artículo científico publicado en 2006

Nuclear matrix involvement in sperm head structural organization.

artículo científico publicado en 1994

Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery–Dreifuss muscular dystrophy patients and carriers

artículo científico publicado en 1998

Pre-Lamin A processing is linked to heterochromatin organization.

artículo científico publicado en 2007

Prelamin A is involved in early steps of muscle differentiation.

artículo científico publicado en 2008

Prelamin A processing and functional effects in restrictive dermopathy

artículo científico publicado en 2010

Prelamin A processing and heterochromatin dynamics in laminopathies.

artículo científico publicado en 2006

Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle.

artículo científico publicado en 2011

Preparation of chromosome spreads for electron (TEM, SEM, STEM), light and confocal microscopy

artículo científico publicado en 1994

Rapamycin treatment of Mandibuloacral dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamics

artículo científico publicado en 2014

Recessive COL6A2 C-globular missense mutations in Ullrich congenital muscular dystrophy: role of the C2a splice variant.

artículo científico publicado en 2010

Reduction of background labeling in colloidal gold-enzyme reactions

artículo científico publicado en 1990

Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment

artículo científico publicado en 2005

Severe wear from retrieved alumina-on-alumina coupled implant: a case report

artículo científico publicado en 2001

Synovial fluid microanalysis allows early diagnosis of ceramic hip prosthesis damage

scientific article published on 27 January 2012

Tendon Extracellular Matrix Remodeling and Defective Cell Polarization in the Presence of Collagen VI Mutations

scientific article published on 11 February 2020

The empowerment of translational research: lessons from laminopathies.

artículo científico publicado en 2012

Ultrastructural changes in muscle cells of patients with collagen VI-related myopathies

scientific article published on October 2013

Ultrastructural defects of collagen VI filaments in an Ullrich syndrome patient with loss of the alpha3(VI) N10-N7 domains

scientific article published on 01 January 2006

Lista de obras de Stefano Squarzoni

82nd ENMC international workshop, 5th international Emery-Dreifuss muscular dystrophy (EDMD) workshop, 1st Workshop of the MYO-CLUSTER project EUROMEN (European muscle envelope nucleopathies), 15-16 September 2000, Naarden, The Netherlands

98th ENMC International Workshop on Congenital Muscular Dystrophy (CMD), 7th Workshop of the International Consortium on CMD, 2nd Workshop of the MYO CLUSTER project GENRE. 26-28th October, 2001, Naarden, The Netherlands.

A case report of fracture of ceramic head in total hip arthroplasty: histological and biochemical features of perimplant tissues

A new method for isolation of polyethylene wear debris from tissue and synovial fluid

A pathogenic mechanism leading to partial lipodistrophy and prospects for pharmacological treatment of insulin resistance syndrome

A recently developed bifacial platelet-rich fibrin matrix

All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype.

Altered chromatin organization and SUN2 localization in mandibuloacral dysplasia are rescued by drug treatment.

Altered pre-lamin A processing is a common mechanism leading to lipodystrophy.

Antisense-induced messenger depletion corrects a COL6A2 dominant mutation in Ullrich myopathy

Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts

At the nucleus of the problem: nuclear proteins and disease

Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria.

Autosomal recessive Bethlem myopathy

Autosomal recessive myosclerosis myopathy is a collagen VI disorder

Barrier-to-autointegration factor (BAF) involvement in prelamin A-related chromatin organization changes

Ceramic debris in hip prosthesis: correlation between synovial fluid and joint capsule

Chromosome spread for confocal microscopy

Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts

Collagen VI-NG2 axis in human tendon fibroblasts under conditions mimicking injury response

Considerations on ceramic prosthesis explants

Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by collagen VI myopathies

Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies

Determination of crystallinity and crystal structure of Hylamer polyethylene after in vivo wear

Differential and restricted expression of novel collagen VI chains in mouse

Diverse lamin-dependent mechanisms interact to control chromatin dynamics. Focus on laminopathies

Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy

Drugs affecting prelamin A processing: effects on heterochromatin organization

Dysferlin in a hyperCKaemic patient with caveolin 3 mutation and in C2C12 cells after p38 MAP kinase inhibition

Early diagnosis of ceramic liner fracture. Guidelines based on a twelve-year clinical experience.

Effect of mechanical strain on the collagen VI pericellular matrix in anterior cruciate ligament fibroblasts.

Effects of prelamin A processing inhibitors on the differentiation and activity of human osteoclasts

Effects on Collagen VI mRNA Stability and Microfibrillar Assembly of ThreeCOL6A2Mutations in Two Families with Ullrich Congenital Muscular Dystrophy

Electron microscopy microsampling of isolated nuclei sorted by flow cytometry

Emerin Phosphorylation during the Early Phase of the Oxidative Stress Response Influences Emerin-BAF Interaction and BAF Nuclear Localization

Emerin increase in regenerating muscle fibers

Emerin presence in platelets

Emerin-prelamin A interplay in human fibroblasts

Emery-Dreifuss muscular dystrophy, nuclear cell signaling and chromatin remodeling

Experimental colitis increases small intestine permeability in the rat

Expression of collagen VI α5 and α6 chains in human muscle and in Duchenne muscular dystrophy-related muscle fibrosis

Expression of the collagen VI α5 and α6 chains in normal human skin and in skin of patients with collagen VI-related myopathies

Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutation

Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for gene transcription

Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistribution

Fretting wear in a modular neck hip prosthesis.

Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy ⬇️

Honey flavonoids inhibit Candida albicans morphogenesis by affecting DNA behavior and mitochondrial function

Image analysis of the chromatin organization in the nuclear domains of freeze fractured hepatocytes and lymphocytes

Image analysis techniques. The problem of the quantitative evaluation of the chromatin ultrastructure

Immunocytochemical detection of emerin within the nuclear matrix

Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology.

Implications for nuclear organization and gene transcription of lamin A/C specific mutations

Increase of Neuronal Nitric Oxide Synthase in Rat Skeletal Muscle during Ageing

Intracellular detection of laminin alpha 2 chain in skin by electron microscopy immunocytochemistry: comparison between normal and laminin alpha 2 chain deficient subjects

Intramembrane protein distribution in cell cultures is affected by 50 Hz pulsed magnetic fields.

Intranuclear localization of phospholipids by ultrastructural cytochemistry

Isolation and characterization of wear debris generated in patients wearing polyethylene Hylamer inserts, gamma irradiated in air.

Lamin A precursor induces barrier-to-autointegration factor nuclear localization

Lamin A/C sustains PcG protein architecture, maintaining transcriptional repression at target genes.

Laminopathies: a chromatin affair

Laminopathies: involvement of structural nuclear proteins in the pathogenesis of an increasing number of human diseases

Localization of laminin alpha 2 chain in normal human central nervous system: an immunofluorescence and ultrastructural study

Localization of the laminin alpha 2 chain in normal human skeletal muscle and peripheral nerve: an ultrastructural immunolabeling study

Metal-on-metal hip prostheses: correlation between debris in the synovial fluid and levels of cobalt and chromium ions in the bloodstream.

Mineralization behavior with mesenchymal stromal cells in a biomimetic hyaluronic acid-based scaffold.

Mixing and matching in ceramic-on-metal hip arthroplasty: an in-vitro hip simulator study

Modulation of TGFbeta 2 levels by lamin A in U2-OS osteoblast-like cells: understanding the osteolytic process triggered by altered lamins

Morphological evidence of function-related localization of phospholipids in the cell nucleus

Morphometric and microanalytical analyses of alumina wear particles in hip prostheses

Morphometric study of chromatin pattern in freeze-fractured rat liver nuclei during malignancy evolution

Muscular laminopathies: role of prelamin A in early steps of muscle differentiation

New roles for lamins, nuclear envelope proteins and actin in the nucleus

Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy

Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophy

Nuclear envelope proteins and chromatin arrangement: a pathogenic mechanism for laminopathies.

Nuclear matrix involvement in sperm head structural organization.

Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery–Dreifuss muscular dystrophy patients and carriers

Pre-Lamin A processing is linked to heterochromatin organization.